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Mn(III)-Based Oxidation of Methoxynaphthalenes with 3-Oxobutanamides
http://hdl.handle.net/2298/12277
http://hdl.handle.net/2298/122775a1885e6-0751-4ff3-86ce-b5a6e49dce0c
| 名前 / ファイル | ライセンス | アクション |
|---|---|---|
KT0017_005-008.pdf (520.4 kB)
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| Item type | 紀要論文 / Departmental Bulletin Paper(1) | |||||
|---|---|---|---|---|---|---|
| 公開日 | 2009-09-08 | |||||
| タイトル | ||||||
| タイトル | Mn(III)-Based Oxidation of Methoxynaphthalenes with 3-Oxobutanamides | |||||
| 言語 | en | |||||
| 言語 | ||||||
| 言語 | eng | |||||
| 資源タイプ | ||||||
| 資源タイプ | departmental bulletin paper | |||||
| 著者 |
Cong, Zhiqi
× Cong, Zhiqi× 西野, 宏 |
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| 内容記述 | ||||||
| 内容記述タイプ | Other | |||||
| 内容記述 | Oxidation of a mixture of 2,7-dimethoxynaphthalene and N-phenyl-3-oxobutanamide with manganese(III) acetate in acetic acid at reflux temperature gave direct 3-oxobutanamide-substituted naphthalene, naphtho[2,1-b]furan and lactam derivatives in moderate yields, respectively. The same procedure could be applied to a combination of other 2-methoxyl substituted naphthalenes with various 3-oxobutanamides, and the homologues were obtained in similar yields. The characterization of the reaction products, the examination of the optimum reaction conditions, and the mechanism for the formation of the products were discussed. | |||||
| 書誌情報 |
ja : 熊本大学極低温装置室ユーザー研究報告書 : 熊大極低温 巻 17, p. 5-8, 発行年 2006-12 |
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| NCID | ||||||
| 収録物識別子タイプ | NCID | |||||
| 収録物識別子 | AA12112448 | |||||
| 著者版フラグ | ||||||
| 出版タイプ | AM | |||||
| 日本十進分類法 | ||||||
| 主題Scheme | NDC | |||||
| 主題 | 436 | |||||
| 出版者 | ||||||
| 出版者 | 熊本大学 | |||||
| 言語 | ja | |||||
| コメント | ||||||
| ja | ||||||
| 文末に Supporting information あり | ||||||
